Disease #01596 (CMH1 (cardiomyopathy, hypertrophic, familial, type 1 (CMH-1)), OMIM:192600)
Official abbreviation |
CMH1 |
Name |
cardiomyopathy, hypertrophic, familial, type 1 (CMH-1) |
OMIM ID |
192600 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Digenic dominant |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 4 genes |
CAV3, MYH6, MYH7, MYLK2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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